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Merck
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34224

Supelco

甲嘧磺隆

PESTANAL®, analytical standard

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About This Item

經驗公式(希爾表示法):
C15H16N4O5S
CAS號碼:
分子量::
364.38
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

格式

neat

SMILES 字串

COC(=O)c1ccccc1S(=O)(=O)NC(=O)Nc2nc(C)cc(C)n2

InChI

1S/C15H16N4O5S/c1-9-8-10(2)17-14(16-9)18-15(21)19-25(22,23)12-7-5-4-6-11(12)13(20)24-3/h4-8H,1-3H3,(H2,16,17,18,19,21)

InChI 密鑰

ZDXMLEQEMNLCQG-UHFFFAOYSA-N

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相關類別

一般說明

Sulfometuron methyl, can be called as one of the few sulfonylurea herbicides with high herbicidal activity. It can inhibit the growth of several bacterial species including Salmonella typhimurium, found in intestinal lumen and can also suppress the growth of yeast like Saccharomyces cerevisiae by blocking acetolactate synthase enzyme.

應用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律資訊

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形圖

Environment

訊號詞

Warning

危險聲明

防範說明

危險分類

Aquatic Acute 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


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分析證明 (COA)

Lot/Batch Number

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Single amino acid substitutions in the enzyme acetolactate synthase confer resistance to the herbicide sulfometuron methyl
Yadav N, et al.
Proceedings of the National Academy of Sciences of the USA, 83, 4418-4422 (1986)
Genetic analysis of mutants of Saccharomyces cerevisiae resistant to the herbicide sulfometuron methyl
Falco.C.S and Dumas.S.K
Genetics, 109, 21-35 (1985)
A Coly et al.
Journal of AOAC International, 84(6), 1745-1750 (2002-01-05)
First-derivative photochemically induced spectrofluorimetry (PIF-1D) is applied to the simultaneous determination of binary mixtures of 4 sulfonylurea herbicides in aqueous micellar samples. Synthetic binary mixtures of sulfometuronmethyl with chlorsulfuron, metsulfuron-methyl, and 3-rimsulfuron, respectively, are well resolved by using the zero-crossing
Yael Golda Mishael et al.
Journal of agricultural and food chemistry, 50(10), 2856-2863 (2002-05-02)
The aim of this study was to understand the interactions between alkylammonium cations present as monomers and micelles and a clay mineral, montmorillonite, to develop slow release formulations of anionic herbicides, such as sulfometuron (SFM) whose leaching in soils is
G Leppert et al.
Genetics, 125(1), 13-20 (1990-05-01)
Yeast DNA fragments that confer multiple drug resistance when amplified were isolated. Cells containing a yeast genomic library cloned in the high copy autonomously replicating vector, YEp24, were plated on medium containing cycloheximide. Five out of 100 cycloheximide-resistant colonies were

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